Medical Device 2012 - Medical Device Regulations and Law in the US, EU and Canada

This 3-hr training will discuss medical device regulations and law in the US, Europe and Canada. It is designed to help the audience with their global compliance and regulatory intelligence, which is necessary to streamline the regulatory process in an organization to achieve sustainability and to remain sustainable and competitive in global markets. This seminar is a “How To Guide” intended to streamline the decision-making process in a systematic manner.

The global regulation of medical devices is rapidly evolving, integrating the regulatory systems of the most advanced medical device regulations. To be able to achieve sustainability and to remain competitive in global medical device markets, it is necessary to streamline the regulatory process what would help to reduce or eliminate differences between countries, gain regulatory compliance at a reduced cost, allow intended users and other stakeholders earlier access to advanced and innovative medical device products for treatments and improve healthcare in a safe and effective way during post-marketing through surveillance program.